Data / Medical devices / China / Quanzhou Aguru E-Commerce Co., Ltd
Quanzhou Aguru E-Commerce Co., Ltd: FDA-registered device maker in Quanzhou Fujian, China, 2 510(k) clearances
Quanzhou Aguru E-Commerce Co., Ltd is registered with the FDA (registration 3042256012) in Quanzhou Fujian, China. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated July 8, 1993. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042256012
- Address
- 1155 Binhai Street, Fengze District Room 1401, Building 5, Phase II of Haichen Zunyu, Quanzhou Fujian, China, 362000
- Owner or operator
- Quanzhou Aguru E-commerce Co., Ltd (10094233)
- Roles
- Manufacturer
- First device listed
- November 19, 2025
- Registered through
- 2026
- Brand names listed
- Plaque Remover for Teeth - Tartar Remover for Teeth, Dental Calculus Remover Teeth Cleaning Kit, Plaque/Tartar Remover for Teeth, Dental Calculus Remover Teeth Cleaning Kit with LED Light & 5 Adjustable Modes
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Scaler, Ultrasonic | ELC | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 8, 1993 | K921893 | COLGATE ODONTOSON ULTRASONIC SCALER | ELC | Substantially Equivalent | Perio-Giene | accessdata.fda.gov |
| April 16, 1991 | K903298 | DYNASONIC PLAQUE REMOVER & POLISHER DYNATIP | ELC | Substantially Equivalent | Micro Motors, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 8, 1993. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.